Some of the software produced by the bioinformatic group at COMAV might be useful from other researchers. We make available with that hope.
ngs_backbone is a bioinformatic application created to work on sequence analysis by using NGS (Next Generation Sequencing) and sanger sequences. It is capable of cleaning reads, do de novo assembly or mapping against a reference and annotate SNPs, SSRs, ORFs, GO terms and sequence descriptions.
clean_reads cleans Next Generation Sequencing reads from the following platforms: 454, Illumina, solid and Sanger.
sff_extract reads the information from the 454 sff files and stores the sequence, quality and adapter clips in fasta and xml files.